MetaADEDB: ADE

MetaADEDB 2.0 @ LMMD

Ketonemia

(UMLS:C0235430)

UMLS ID:: C0235430
MeSH ID:: D007662

Classification:

Name:

Nutritional and Metabolic Diseases
MeSH Tree Number(s):: C18.452.076.176.652

Synonym(s)

Ketonemia

Hyperketonemia

Increased level of ketone bodies in blood

KETONEMIA

Ketonaemia

Serum ketone concentration above normal range

Serum ketones increased

ketonaemia

ketonemia

Associated Drug(s)

	Name	Number of Reports	Reference(s)	Data Source
1	Metformin			SIDER

Similar ADE(s)

	Name	Semantic Similarity
1	Acidosis, Lactic	48.4%
2	Alkalosis	34.4%
3	Acidosis, Respiratory	32.6%
4	Calcium Metabolism Disorders	25.4%
5	Iron Metabolism Disorders	25.4%
6	Phosphorus Metabolism Disorders	25.4%
7	Water-Electrolyte Imbalance	25.4%
8	Lipid Metabolism Disorders	25.4%
9	Mitochondrial Diseases	25.4%
10	Glucose Metabolism Disorders	25.4%
11	Achlorhydria	23.1%
12	Wasting Syndrome	23%
13	Hypercalcemia	19.8%
14	Hypocalcemia	19.8%
15	Milk-Alkali Syndrome	19.8%
16	Renal tubular acidosis	19.3%
17	Osteopenia	17.2%
18	Brain Diseases, Metabolic	16.9%
19	Nutrition Disorders	16.4%
20	Alkalosis, Respiratory	15.2%
21	Lipodystrophy	14.9%
22	Amyloidosis	14.8%
23	Calcinosis	14.8%
24	Hyperglycemia	14.8%
25	Hyperinsulinism	14.8%
26	Hyperkalemia	14.8%
27	Hypernatremia	14.8%
28	Hypoglycemia	14.8%
29	Hypokalemia	14.8%
30	Hyponatremia	14.8%
31	Xanthomatosis	14.8%
32	Hypophosphatemia	14.8%
33	Dyslipidemias	14.8%
34	Iron Overload	14.8%
35	Xanthoma	14.8%
36	Pseudohypoparathyroidism	13.1%
37	Rickets	12.6%
38	Brain Diseases, Metabolic, Inborn	11.8%
39	Diabetes Mellitus	10.6%
40	Hyperhomocysteinemia	10.5%
41	Leigh Disease	10.3%
42	Dehydration	10.1%
43	Lipomatosis	10.1%
44	Water Intoxication	10.1%
45	Werner Syndrome	10.1%
46	Amino Acid Metabolism, Inborn Errors	9.9%
47	Bloom Syndrome	9.9%
48	Carbohydrate Metabolism, Inborn Errors	9.9%
49	Metal Metabolism, Inborn Errors	9.9%
50	Osteoporosis	9.9%
51	Progeria	9.9%
52	Lysosomal Storage Diseases	9.9%
53	Bone Demineralization, Pathologic	9.9%
54	Cytochrome-c Oxidase Deficiency	9.9%
55	Peroxisomal Disorders	9.9%
56	Post-Traumatic Osteoporosis	9.9%
57	Celiac Disease	9.8%
58	Sprue, Tropical	9.8%
59	Steatorrhea	9.8%
60	Sprue	9.8%
61	Lactose Intolerance	9.7%
62	Calciphylaxis	9.7%
63	Hemosiderosis	9.7%
64	Hypolipoproteinemias	9.7%
65	Vascular calcification	9.7%
66	Carbamoyl-Phosphate Synthase I Deficiency Disease	9%
67	Hyperlipoproteinemia Type IV	8.6%
68	Hyperlipoproteinemia Type V	8.6%
69	Child Nutrition Disorders	8.5%
70	Hypervitaminosis A	8.5%
71	Infant Nutrition Disorders	8.5%
72	Malnutrition	8.5%
73	Hyperlipidemia, Familial Combined	8.4%
74	Osteomalacia	8.4%
75	Smith-Lemli-Opitz Syndrome	8.3%
76	Galactosemias	8.3%
77	Urea Cycle Disorders, Inborn	8.3%
78	Tyrosinemias	8.3%
79	Mitochondrial Encephalomyopathies	8.2%
80	Congenital Hyperinsulinism	8.1%
81	Hyperlipoproteinemia Type III	7.8%
82	Mitochondrial Myopathies	7.6%
83	Myelinolysis, Central Pontine	7.5%
84	Glycosuria	7.4%
85	Reye Syndrome	7.4%
86	Hepatic Encephalopathy	7.3%
87	Hyperphosphaturia	7.2%
88	Hypercholesterolemia	7.2%
89	Hyperlipoproteinemias	7.2%
90	Hypertriglyceridemia	7.2%
91	Hypoalphalipoproteinemias	7.2%
92	Familial Hypophosphatemic Rickets	6.8%
93	Homocystinuria	6.7%
94	HIV Wasting Syndrome	6.5%
95	Adiposis Dolorosa	6.5%
96	Alkaptonuria	6.5%
97	Glycogen Storage Disease	6.5%
98	Hypophosphatasia	6.5%
99	Insulin Resistance	6.5%
100	Osteoporosis, Postmenopausal	6.5%
101	Propionic acidemia	6.5%
102	Dihydropyrimidine Dehydrogenase Deficiency	6.5%
103	Cystinosis	6.5%
104	Glycogen storage disease type II	6.4%
105	Gaucher Disease	6.2%
106	Amyloid Neuropathies, Familial	6.1%
107	Porphyrias, Hepatic	6%
108	Necrobiosis Lipoidica Diabeticorum	5.9%
109	Fanconi Anemia	5.8%
110	Nesidioblastosis	5.8%
111	Neuronal Ceroid-Lipofuscinoses	5.7%
112	HIV-Associated Lipodystrophy Syndrome	5.5%
113	Wernicke Encephalopathy	5.5%
114	Zellweger Syndrome	5.3%
115	Renal Osteodystrophy	5.3%
116	Renal rickets	5.3%
117	MELAS Syndrome	5.3%
118	Menkes Kinky Hair Syndrome	5.3%
119	Adrenoleukodystrophy	5.1%
120	Gestational Diabetes	5.1%
121	Latent Autoimmune Diabetes in Adults	5.1%
122	Tay-Sachs Disease	5.1%
123	Diabetes Mellitus, Experimental	5%
124	Niemann-Pick Disease, Type C	4.9%
125	Deficiency Diseases	4.9%
126	Starvation	4.9%
127	Refeeding Syndrome	4.9%
128	Hepatolenticular Degeneration	4.9%
129	Nephrocalcinosis	4.9%
130	Tetany	4.9%
131	Diabetic Ketoacidosis	4.9%
132	Friedreich Ataxia	4.9%
133	Refsum Disease	4.8%
134	Glycosuria, Renal	4.8%
135	Cerebral Amyloid Angiopathy	4.8%
136	Glycogen Storage Disease Type I	4.8%
137	Glycogen Storage Disease Type V	4.8%
138	Mucopolysaccharidosis III	4.8%
139	Fabry Disease	4.8%
140	Kernicterus	4.3%
141	Cockayne Syndrome	4.2%
142	Familial Periodic Paralysis	4%
143	Primary amyloidosis	3.9%
144	Kearns-Sayre syndrome	3.9%
145	Variegate Porphyria	3.9%
146	Acute intermittent porphyria	3.9%
147	Porphyria Cutanea Tarda	3.9%
148	Renal Aminoacidurias	3.9%
149	Fanconi Syndrome	3.9%
150	Pseudohypoaldosteronism	3.9%
151	Liddle Syndrome	3.9%
152	Ataxia Telangiectasia	3.8%
153	Optic Atrophy, Hereditary, Leber	3.7%
154	Sjogren-Larsson Syndrome	3.4%
155	Xeroderma Pigmentosum	3.3%
156	Gout	3.3%
157	Amyotrophic Lateral Sclerosis	3.3%
158	Antley-Bixler Syndrome Phenotype	3.2%
159	Canavan Disease	3.2%
160	Alexander Disease	3.2%
161	Kwashiorkor	3.2%
162	Magnesium Deficiency	3.2%
163	Potassium Deficiency	3.2%
164	Protein Deficiency	3.2%
165	Avitaminosis	3.2%
166	Mucopolysaccharidosis II	3.2%
167	Hypokalemic periodic paralysis	2.9%
168	Frontotemporal dementia	2.9%
169	Cystinuria	2.9%
170	CREST Syndrome	2.8%
171	Albinism	2.5%
172	Arthritis, Gouty	2.4%
173	Ascorbic Acid Deficiency	2.4%
174	Vitamin A Deficiency	2.4%
175	Vitamin D Deficiency	2.4%
176	Vitamin E Deficiency	2.4%
177	Marasmus	2.4%
178	Folic Acid Deficiency	2%
179	Pellagra	2%
180	Thiamine Deficiency	2%
181	Vitamin B 12 Deficiency	2%
182	Vitamin B 6 Deficiency	2%
183	Pyridoxine Deficiency	2%
184	Ichthyosis, X-Linked	2%
185	Obesity	1.9%
186	Beriberi	1.8%
187	Obesity, Abdominal	1.6%
188	Pediatric Obesity	1.3%
189	Vitamin K Deficiency	1.2%
190	Anemia, Pernicious	1.2%
191	Prader-Willi Syndrome	1.1%
192	Scurvy	1%
193	Subacute Combined Degeneration	0.6%

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